New Horizons of Synthetic Lethality in Cancer: Current Development and Future Perspectives

被引:11
|
作者
Previtali, Viola [1 ]
Bagnolini, Greta [2 ]
Ciamarone, Andrea [1 ,2 ]
Ferrandi, Giovanni [1 ,2 ]
Rinaldi, Francesco [1 ]
Myers, Samuel Harry [1 ]
Roberti, Marinella [2 ]
Cavalli, Andrea [1 ,2 ,3 ]
机构
[1] Ist Italiano Tecnol, Computat & Chem Biol, I-16163 Genoa, Italy
[2] Univ Bologna, Dept Pharm & Biotechnol, I-40126 Bologna, Italy
[3] Ecole Polytech Fed Lausanne, CECAM, Ave Forel 3, CH-1015 Lausanne, Switzerland
关键词
HOMOLOGOUS-RECOMBINATION-DEFICIENT; DNA-POLYMERASE-THETA; SELECTIVE WEE1 INHIBITOR; PROTEIN-KINASE; RAD52; INACTIVATION; ANTITUMOR-ACTIVITY; BREAST-CANCER; DRUG TARGET; POL-THETA; ATR;
D O I
10.1021/acs.jmedchem.4c00113
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In recent years, synthetic lethality has been recognized as a solid paradigm for anticancer therapies. The discovery of a growing number of synthetic lethal targets has led to a significant expansion in the use of synthetic lethality, far beyond poly(ADP-ribose) polymerase inhibitors used to treat BRCA1/2-defective tumors. In particular, molecular targets within DNA damage response have provided a source of inhibitors that have rapidly reached clinical trials. This Perspective focuses on the most recent progress in synthetic lethal targets and their inhibitors, within and beyond the DNA damage response, describing their design and associated therapeutic strategies. We will conclude by discussing the current challenges and new opportunities for this promising field of research, to stimulate discussion in the medicinal chemistry community, allowing the investigation of synthetic lethality to reach its full potential.
引用
收藏
页码:11488 / 11521
页数:34
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